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Expression of S100A10 gene and its regulation by sex hormones in mouse uterus

机译:S100A10基因在小鼠子宫中的表达及其性激素的调控

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摘要

S100A10 belongs to the S100 calcium binding protein superfamily, and functions as one of the mediators of calcium-de-pendent signaling pathway. Recently, S100A10 gene was proved to be significantly up-regulated at the implantation site. In the present study, semi-quantitative reverse transcriptase-polymerase chain reaction and in situ hybridization are used to investigate the tissue-specificity of S100A10 expression and the expression pattern of S100A10 in the uteri during the estrous cycle and pregnancy. Meanwhile, the regulation of S100A10 expression by sex steroid hormones is studied in ovariectomized mice. The results show that S100A10 could be detected in various kinds of tissues, with relatively high expression in reproductive tracts including ovary, uterus, testis and epididyrnis. During pregnancy, the expression of S100A10 in the uteri is significantly up-regulated on the 4th day. The transcript is strongly detected in endometrial stromal cells and weakly in luminal epithelium cells at theimplantation site, but almost not at the inter-implantation site. From gestational day 5 till labor, S100A10 mRNA maintains a certain level in both uteri and placentae. During the estrous cycle, expression of S100A10 is up-regulated in the uteri at proestrus and estrus. Estradiol significantly induces the expression of S100A10, while progesterone can abolish the effect of estradiol. The data suggests that S100A10 may be involved in preventing luminal epithelial cells from over-apoptosis, inducing proliferation and decidualization of stromal cells during implantation, and responding to reproductive stress triggered by copulation.
机译:S100A10属于S100钙结合蛋白超家族,是钙依赖型信号通路的介质之一。最近,S100A10基因被证明在植入部位明显上调。在本研究中,使用半定量逆转录酶-聚合酶链反应和原位杂交来研究在发情周期和妊娠期子宫内S100A10表达的组织特异性和子宫中S100A10的表达模式。同时,在去卵巢小鼠中研究了性类固醇激素对S100A10表达的调节。结果表明,可以在各种组织中检测到S100A10,并且在包括卵巢,子宫,睾丸和附睾的生殖道中表达较高。在怀孕期间,子宫内S100A10的表达在第4天显着上调。转录物在子宫内膜间质细胞中被强烈检测到,而在腔内上皮细胞中则被检测到较弱,而在植入间位置则几乎没有。从妊娠第5天到分娩,S100A10 mRNA在子宫和胎盘中均保持一定水平。在发情周期中,S100A10的表达在发情期和发情期子宫中上调。雌二醇可明显诱导S100A10的表达,而孕酮可消除雌二醇的作用。数据表明,S100A10可能参与防止腔上皮细胞过度凋亡,在植入过程中诱导基质细胞增殖和蜕膜化,以及应对交配引发的生殖压力。

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